메뉴 건너뛰기




Volumn 53, Issue 5, 2004, Pages 756-758

Iron chelation therapy in aceruloplasminaemia: Study of a patient with a novel missense mutation

Author keywords

[No Author keywords available]

Indexed keywords

C REACTIVE PROTEIN; CERULOPLASMIN; DEFERIPRONE; FERRITIN; IRON CHELATING AGENT; PHENYLALANINE; TRANSFERRIN;

EID: 2342434172     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.2003.030429     Document Type: Article
Times cited : (51)

References (15)
  • 1
    • 0032579397 scopus 로고    scopus 로고
    • Role of ceruloplasmin in cellular iron uptake
    • Mukhopadhayay CK, Attieh ZK, Fox PL. Role of ceruloplasmin in cellular iron uptake. Science 1998;279:714-17.
    • (1998) Science , vol.279 , pp. 714-717
    • Mukhopadhayay, C.K.1    Attieh, Z.K.2    Fox, P.L.3
  • 2
    • 0032875387 scopus 로고    scopus 로고
    • Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux
    • Harris ZL, Durley AP, Man TK, et al. Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux. Proc Natl Acad Sci U S A 1999;96:10812-17.
    • (1999) Proc Natl Acad Sci U S A , vol.96 , pp. 10812-10817
    • Harris, Z.L.1    Durley, A.P.2    Man, T.K.3
  • 3
    • 0036800145 scopus 로고    scopus 로고
    • The copper-iron connection: Hereditary aceruloplasminemia
    • Nittis T, Gitlin JD. The copper-iron connection: hereditary aceruloplasminemia. Semin Hematol 2002;39:282-9.
    • (2002) Semin Hematol , vol.39 , pp. 282-289
    • Nittis, T.1    Gitlin, J.D.2
  • 4
    • 0032843885 scopus 로고    scopus 로고
    • A case of hereditary ceruloplasmin deficiency with iron deposition in the brain associated with chorea, dementia, diabetes mellitus and retinal pigmentation: Administration of fresh-frozen human plasma
    • Yonekawa M, Okabe T, Asamoto Y, et al. A case of hereditary ceruloplasmin deficiency with iron deposition in the brain associated with chorea, dementia, diabetes mellitus and retinal pigmentation: administration of fresh-frozen human plasma. Eur Neurol 1999;42:157-62.
    • (1999) Eur Neurol , vol.42 , pp. 157-162
    • Yonekawa, M.1    Okabe, T.2    Asamoto, Y.3
  • 5
    • 0029007765 scopus 로고
    • Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study or a Japanese family
    • Morita H, Ikeda S, Yamamoto K, et al. Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study or a Japanese family. Ann Neurol 1995;37:646-56.
    • (1995) Ann Neurol , vol.37 , pp. 646-656
    • Morita, H.1    Ikeda, S.2    Yamamoto, K.3
  • 6
    • 0037105376 scopus 로고    scopus 로고
    • Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations
    • Bosio S, De Gobbi M, Roetto A, et al. Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations. Blood 2002;100:2246-8.
    • (2002) Blood , vol.100 , pp. 2246-2248
    • Bosio, S.1    De Gobbi, M.2    Roetto, A.3
  • 7
    • 0036623360 scopus 로고    scopus 로고
    • Aceruloplasminemia: New clinical, pathophysiological and therapeutic insights
    • Lorèal O, Turlin B, Pigeon C, et al. Aceruloplasminemia: new clinical, pathophysiological and therapeutic insights. J Hepatol 2002;36:851-6.
    • (2002) J Hepatol , vol.36 , pp. 851-856
    • Lorèal, O.1    Turlin, B.2    Pigeon, C.3
  • 8
    • 0033665697 scopus 로고    scopus 로고
    • Hepatic iron overload in aceruloplasminemia
    • Helman NE, Schafer M, Gehrke S, et al. Hepatic iron overload in aceruloplasminemia. Gut 2000;47:858-60.
    • (2000) Gut , vol.47 , pp. 858-860
    • Helman, N.E.1    Schafer, M.2    Gehrke, S.3
  • 9
    • 0031058837 scopus 로고    scopus 로고
    • Use of desferrioxamine in the treatment of aceruloplasminemia
    • Miyajima H, Takahashi Y, Kamats T, et al. Use of desferrioxamine in the treatment of aceruloplasminemia. Ann Neurol 1997;41:404-7.
    • (1997) Ann Neurol , vol.41 , pp. 404-407
    • Miyajima, H.1    Takahashi, Y.2    Kamats, T.3
  • 11
    • 0020465049 scopus 로고
    • Magnetic-susceptibility measurement of human iron stores
    • Brittenham GM, Forrell DE, Harris JW, et al. Magnetic-susceptibility measurement of human iron stores. N Engl J Med 1982;307:1671-5.
    • (1982) N Engl J Med , vol.307 , pp. 1671-1675
    • Brittenham, G.M.1    Forrell, D.E.2    Harris, J.W.3
  • 12
    • 0035206994 scopus 로고    scopus 로고
    • A study of genes that may modulate the expression of hereditary hemochromatosis: Transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chain, iron regulatory proteins (IRP)-1 and -2, and hepcidin
    • Lee PL, Gelbart T, West C, et al. A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chain, iron regulatory proteins (IRP)-1 and -2, and hepcidin. Blood Cell Mol Dis 2001;27:783-802.
    • (2001) Blood Cell Mol Dis , vol.27 , pp. 783-802
    • Lee, P.L.1    Gelbart, T.2    West, C.3
  • 13
    • 0037059741 scopus 로고    scopus 로고
    • Biochemical analysis of a missense mutation in aceruloplasminemia
    • Hellman NE, Kono S, Miyajima H, et al. Biochemical analysis of a missense mutation in aceruloplasminemia. J Biol Chem 2002;277:1375-80.
    • (2002) J Biol Chem , vol.277 , pp. 1375-1380
    • Hellman, N.E.1    Kono, S.2    Miyajima, H.3
  • 14
    • 0032984353 scopus 로고    scopus 로고
    • Hypocaeruloplasminemia with heteroallelic caeruloplasmin gene mutation: MRI of the brain
    • Daiman M, Morial S, Susa A, et al. Hypocaeruloplasminemia with heteroallelic caeruloplasmin gene mutation: MRI of the brain. Neuroradiology 1999;41:185-7.
    • (1999) Neuroradiology , vol.41 , pp. 185-187
    • Daiman, M.1    Morial, S.2    Susa, A.3
  • 15
    • 0035956555 scopus 로고    scopus 로고
    • Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation
    • Miyajima H, Kono S, Takahashi Y, et al. Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation. Neurology 2001;57:2205-10.
    • (2001) Neurology , vol.57 , pp. 2205-2210
    • Miyajima, H.1    Kono, S.2    Takahashi, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.